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A General and Long-Lived Catalyst for the Palladium-Catalyzed Coupling of Aryl Halides with Thiols
696
Citations
9
References
2006
Year
Palladium-catalyzed CouplingChemical EngineeringAryl HalidesHydrogen Sulfide SurrogateEngineeringAlkene MetathesisCross-coupling ReactionGeneral Catalytic SystemAryl SulfidesOrganic ChemistryOrganometallic CatalysisCatalysisChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisLong-lived Catalyst
A general catalytic system for the coupling of aryl halides and sulfonates with thiols based on the use of the CyPF-t-Bu ligand (1) is reported. The reactions catalyzed by complexes of 1 occur in excellent yields with broad scope and exhibit extraordinary turnover numbers and high tolerance of functional groups. Turnover numbers usually exceed those of previous catalysts by 2 or 3 orders of magnitude. In addition, the reactions of aryl tosylates with alkane thiols to form aryl sulfides are reported for the first time. Finally, the synthesis of a diarylsulfide from two bromoarenes was accomplished using a hydrogen sulfide surrogate.
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